Clean Room Rabs

A controlled and aseptic production environment is essential in the pharmaceutical and biotech industry, and Kirhtech-NetSteril’s RABS (Restricted Access Barrier Systems) provide this.

These systems ensure the integrity and quality of the processes being carried out and the products handled inside by combining high-efficiency laminar airflow with physical barriers, thereby minimizing the risk of microbial contamination.

At Kirhtech, we collaborate with Netsteril, a company that specializes in the supply and distribution of aseptic process solutions, VH2O2 bio-decontamination services and systems, and glove integrity testing and transfer systems (RTP and beta-containers), to develop our RABS technology.

Characteristics in general

Structure: Constructed from sanitary finishes and AISI 304/316L stainless steel, this item provides both durability and resistance to corrosion. Custom ergonomic design with mock-up review to optimize personnel operations.
Dimensions: Flexible to accommodate the requirements of customers, ranging from small-scale units to large-scale systems.
Panels: acrylic, tempered, or laminated glass panels that are either hinged or fixed to ensure the process is visible to the fullest.
MK® Gloves and GIT (Glove Integrity Test) equipment: Ergonomic ports are intended to ensure the integrity of the glove assembly and the integrity of the integrity test equipment, which is equipped with validated recipes for each glove type. Glove extenders are necessary to ensure adequate exposure during the biodecontamination process.
Lamiar airflow: Indoors, guaranteeing ISO 5 conditions in accordance with ISO 14644-1 or Class A in accordance with GMP, the flow is unidirectional downward at 0.45 m/s ± 20%.
Air treatment: Passive (connected to the room HVAC) or active (equipped with HEPA filters and fans) systems.